ClinVar Miner

List of variants in gene KRAS studied for cancer

Included ClinVar conditions (475):
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Gene type:
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Total variants: 117
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HGVS dbSNP gnomAD frequency
NM_033360.4(KRAS):c.5-18A>G rs200189105 0.00100
NM_004985.5(KRAS):c.24A>G (p.Val8=) rs147406419 0.00025
NM_033360.4(KRAS):c.90C>T (p.Asp30=) rs113623140 0.00011
NM_033360.4(KRAS):c.4+5G>A rs201789109 0.00006
NM_004985.5(KRAS):c.451-5652C>T rs727505314 0.00004
NM_033360.4(KRAS):c.389C>T (p.Ala130Val) rs730880473 0.00002
NM_004985.5(KRAS):c.34G>A (p.Gly12Ser) rs121913530 0.00001
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp) rs121913529 0.00001
NM_004985.5(KRAS):c.38G>A (p.Gly13Asp) rs112445441 0.00001
NM_004985.5(KRAS):c.437C>T (p.Ala146Val) rs1057519725 0.00001
NM_004985.5(KRAS):c.57G>C (p.Leu19Phe) rs121913538 0.00001
NM_033360.4(KRAS):c.112-5C>T rs376520586 0.00001
NM_004985.5(KRAS):c.-10C>G
NM_004985.5(KRAS):c.-11-10T>G
NM_004985.5(KRAS):c.-11-12T>A
NM_004985.5(KRAS):c.-11-12T>G
NM_004985.5(KRAS):c.-11-1G>C
NM_004985.5(KRAS):c.-11-21T>G
NM_004985.5(KRAS):c.-11-2A>C
NM_004985.5(KRAS):c.-11-2A>T
NM_004985.5(KRAS):c.-11-36C>T
NM_004985.5(KRAS):c.-11-4T>A
NM_004985.5(KRAS):c.-11-51del
NM_004985.5(KRAS):c.-11-7T>A
NM_004985.5(KRAS):c.-11-8A>C
NM_004985.5(KRAS):c.-11-8_-11-7insC
NM_004985.5(KRAS):c.-11G>A
NM_004985.5(KRAS):c.-6C>T
NM_004985.5(KRAS):c.101C>G (p.Pro34Arg) rs104894366
NM_004985.5(KRAS):c.107T>A (p.Ile36Lys)
NM_004985.5(KRAS):c.108delinsCC (p.Glu37fs)
NM_004985.5(KRAS):c.109G>T (p.Glu37Ter)
NM_004985.5(KRAS):c.109_110insC (p.Glu37fs)
NM_004985.5(KRAS):c.10T>A (p.Tyr4Asn)
NM_004985.5(KRAS):c.111+11T>C
NM_004985.5(KRAS):c.111+14del
NM_004985.5(KRAS):c.111+16A>G
NM_004985.5(KRAS):c.111+1G>C
NM_004985.5(KRAS):c.111+24A>G
NM_004985.5(KRAS):c.111+25T>C
NM_004985.5(KRAS):c.111+28C>T
NM_004985.5(KRAS):c.111+30G>T
NM_004985.5(KRAS):c.111+50T>A
NM_004985.5(KRAS):c.111+53A>G
NM_004985.5(KRAS):c.111+6T>C
NM_004985.5(KRAS):c.111+8T>C
NM_004985.5(KRAS):c.112-9C>T rs727504298
NM_004985.5(KRAS):c.11A>T (p.Tyr4Phe)
NM_004985.5(KRAS):c.12T>A (p.Tyr4Ter)
NM_004985.5(KRAS):c.13A>G (p.Lys5Glu) rs193929331
NM_004985.5(KRAS):c.13A>T (p.Lys5Ter)
NM_004985.5(KRAS):c.16C>T (p.Leu6Phe)
NM_004985.5(KRAS):c.179G>T (p.Gly60Val) rs727503108
NM_004985.5(KRAS):c.181C>A (p.Gln61Lys) rs121913238
NM_004985.5(KRAS):c.182A>G (p.Gln61Arg) rs121913240
NM_004985.5(KRAS):c.182A>T (p.Gln61Leu) rs121913240
NM_004985.5(KRAS):c.183A>C (p.Gln61His) rs17851045
NM_004985.5(KRAS):c.183A>T (p.Gln61His) rs17851045
NM_004985.5(KRAS):c.1del (p.Met1*)
NM_004985.5(KRAS):c.21_22insT (p.Val8fs)
NM_004985.5(KRAS):c.24dup (p.Val9fs)
NM_004985.5(KRAS):c.27T>A (p.Val9=)
NM_004985.5(KRAS):c.27T>G (p.Val9=)
NM_004985.5(KRAS):c.27_28insCTC (p.Val9_Gly10insLeu)
NM_004985.5(KRAS):c.290G>A (p.Arg97Lys) rs727503106
NM_004985.5(KRAS):c.291-50A>G rs1951385786
NM_004985.5(KRAS):c.29_30insT (p.Ala11fs)
NM_004985.5(KRAS):c.29_31del (p.Gly10del)
NM_004985.5(KRAS):c.30A>G (p.Gly10=) rs2135806293
NM_004985.5(KRAS):c.31G>T (p.Ala11Ser)
NM_004985.5(KRAS):c.33T>A (p.Ala11=)
NM_004985.5(KRAS):c.34G>C (p.Gly12Arg) rs121913530
NM_004985.5(KRAS):c.34G>T (p.Gly12Cys) rs121913530
NM_004985.5(KRAS):c.35G>C (p.Gly12Ala) rs121913529
NM_004985.5(KRAS):c.35G>T (p.Gly12Val) rs121913529
NM_004985.5(KRAS):c.37G>C (p.Gly13Arg) rs121913535
NM_004985.5(KRAS):c.37G>T (p.Gly13Cys) rs121913535
NM_004985.5(KRAS):c.388_389delinsAT (p.Ala130Ile) rs1951383854
NM_004985.5(KRAS):c.38G>T (p.Gly13Val) rs112445441
NM_004985.5(KRAS):c.39C>A (p.Gly13=) rs397517040
NM_004985.5(KRAS):c.39C>T (p.Gly13=) rs397517040
NM_004985.5(KRAS):c.40G>A (p.Val14Ile) rs104894365
NM_004985.5(KRAS):c.42A>T (p.Val14=)
NM_004985.5(KRAS):c.43G>T (p.Gly15Cys)
NM_004985.5(KRAS):c.445A>T (p.Arg149Ter) rs2141505552
NM_004985.5(KRAS):c.458A>T (p.Asp153Val) rs104894360
NM_004985.5(KRAS):c.4del (p.Thr2fs)
NM_004985.5(KRAS):c.50G>T (p.Ser17Ile)
NM_004985.5(KRAS):c.5C>G (p.Thr2Ser)
NM_004985.5(KRAS):c.62T>A (p.Ile21Lys)
NM_004985.5(KRAS):c.65A>C (p.Gln22Pro)
NM_004985.5(KRAS):c.65A>G (p.Gln22Arg) rs727503110
NM_004985.5(KRAS):c.6T>G (p.Thr2=)
NM_004985.5(KRAS):c.74A>T (p.Gln25Leu)
NM_004985.5(KRAS):c.75G>A (p.Gln25=)
NM_004985.5(KRAS):c.77A>C (p.Asn26Thr)
NM_004985.5(KRAS):c.80A>G (p.His27Arg)
NM_004985.5(KRAS):c.80A>T (p.His27Leu)
NM_004985.5(KRAS):c.84T>A (p.Phe28Leu)
NM_004985.5(KRAS):c.84del (p.Phe28fs)
NM_004985.5(KRAS):c.90C>A (p.Asp30Glu)
NM_004985.5(KRAS):c.91G>T (p.Glu31Ter)
NM_004985.5(KRAS):c.95A>C (p.Tyr32Ser)
NM_004985.5(KRAS):c.99T>C (p.Asp33=)
NM_004985.5(KRAS):c.9dup (p.Tyr4fs)
NM_033360.4(KRAS):c.*101_*106del rs1339924833
NM_033360.4(KRAS):c.-11delG
NM_033360.4(KRAS):c.176C>T (p.Ala59Val) rs104886029
NM_033360.4(KRAS):c.216G>A (p.Met72Ile) rs104886028
NM_033360.4(KRAS):c.219G>A (p.Arg73=) rs104886027
NM_033360.4(KRAS):c.27_29dup (p.Gly10dup) rs606231202
NM_033360.4(KRAS):c.351A>C (p.Lys117Asn) rs770248150
NM_033360.4(KRAS):c.355G>A (p.Asp119Asn) rs730880471
NM_033360.4(KRAS):c.37G>A (p.Gly13Ser) rs121913535
NM_033360.4(KRAS):c.38G>C (p.Gly13Ala) rs112445441
NM_033360.4(KRAS):c.436G>C (p.Ala146Pro) rs121913527
NM_033360.4(KRAS):c.57G>T (p.Leu19Phe) rs121913538

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